Capstone: central and peripheral stroke inflammation with exosomes

Active Project Grant Awarded Last action

Award ID
R01NS128425
Recipient
Awarding agency
Obligated
$3,302,589

Award facts

Completion date 72% complete
Originally
Place of performance
Cincinnati, OH 45219, USA

Award details come from USAspending.gov.

Description

Abstract
Intracerebral hemorrhage (ICH) is a severe neurological disorder with no proven treatment. There is increasing evidence that inflammation contributes to ICH outcomes, but the underlying mechanisms remain largely unknown. ICH disproportionately affects ethnic/racial minorities and young people. Our preliminary data confirms reports that ICH survivors have a high rate of progressive cognitive decline, plausibly initiated by the aggressive ICH inflammatory response. Exosomes are extracellular vesicles released from cells into the circulating blood; by analyzing exosomes released from neurons and microglia, brain-specific inflammatory pathophysiology can be assessed by testing circulating plasma. Exosomes transport microrna (mirna) that are powerful regulators of gene expression. In our preliminary studies, three inflammatory mediators emerged as particularly salient in post-ICH inflammation and promising for additional analysis in a larger study: monocytes, interleukin-8 (IL-8), and mirna (MIR)-181A. We propose the capstone (central and peripheral stroke inflammation with exosomes) study that will enroll 250 ICH subjects previously recruited into the rose-lawn study (recovery of stroke, longitudinal assessment with neuroimaging, R01NS120493). Capstone will utilize plasma, peripheral blood, and functional/cognitive outcomes from rose-lawn; serial plasma and blood samples will be analyzed from baseline, three months, and 18 months after ICH. Through the following aims, we will pursue our overall goal to identify transcriptomic biomarkers associated with six-month functional outcome and long-term progressive cognitive decline. Specific aim 1 will determine mirna in neuronal- and microglial-derived exosomes that correlate with six-month functional outcome and long- term progressive cognitive decline (~24 months after ICH). We hypothesize that decreased MIR-181A in neuronal and microglial exosomes will predict worse near-term functional outcome and greater long-term cognitive decline. Specific aim 2 will determine mrna and mirna in peripheral leukocytes that correlate with six-month functional outcome and long-term progressive cognitive decline (~24 months after ICH). We hypothesize that decreased MIR-181A and increased CXCL8 and IL-8 will predict worse functional outcome and greater long-term cognitive decline. Specific aim 3 will explore the interactions between central and peripheral inflammatory processes post-ICH. We hypothesize that decreased MIR-181A in neuronal- and microglial-derived exosomes will be associated with increased CXCL8 and IL-8 from peripheral leukocytes. Post-ICH inflammation is an interplay of both brain-derived and systemic pathology, but the associated molecular mechanisms remain poorly understood. By analyzing circulating blood (i.e., systemic) and cell-specific exosomes in plasma (i.e., brain derived), capstone seeks to provide substantial insight regarding these inflammatory processes. This research also addresses the ninds priorities of recovery, imaging, and vascular cognitive impairment.

Transactions

Action Obligated Date
Amendment $627,689
Amendment $0
Amendment $627,689
Amendment $627,689
Amendment $643,189
Amendment $133,144
Original award $643,189

Subawards

Subrecipient Amount Awarded
Wake Forest University Health Sciences Amend 5 - Biostatistical and Bioinformatic Analysis for CAPSTONE R01 $276,546
The Research Foundation For The State University Of New York Amend 1 - CAPSTONE Central And Peripheral STrOke inflammatioN with Exosomes $14,500
Wake Forest University Health Sciences Amend 3 - Biostatistical and Bioinformatic Analysis for CAPSTONE R01 $86,862
The Research Foundation For The State University Of New York CAPSTONE: Central And Peripheral STrOke inflammatioN with Exosomes $14,847
University Of Vermont & State Agricultural College Amendment #1 $73,114
Wake Forest University Health Sciences $123,545

Quick answers

Who received award R01NS128425?

R01NS128425 was awarded to Cincinnati Univ Of by National Institute of Neurological Disorders and Stroke (National Institutes of Health) on July 19, 2022.

How much is award R01NS128425 worth?

$3,302,589 has been obligated on R01NS128425.

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